Skip to main content

4-chloro-2,3-diiodo-2-buten-1-ol

ADVERTISEMENT
Identification
Molecular formula
C4H5ClI2O
CAS number
947604-63-5
IUPAC name
4-chloro-2,3-diiodo-but-2-en-1-ol
State
State

At room temperature, 4-chloro-2,3-diiodo-2-buten-1-ol is typically found in a solid state due to its relatively high molar mass and strong intermolecular forces exerted by halogen atoms.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
234.00
Boiling point (Kelvin)
507.15
General information
Molecular weight
339.32g/mol
Molar mass
339.3170g/mol
Density
2.6540g/cm3
Appearence

The compound is a crystalline solid. It may exhibit a color ranging from white to pale yellow due to the presence of iodine atoms, which are characteristically heavy and can influence the compound's coloration. It may also have a distinctive odor depending on its purity and specific formulation.

Comment on solubility

Solubility of 4-chloro-2,3-diiodo-but-2-en-1-ol

The solubility of 4-chloro-2,3-diiodo-but-2-en-1-ol can be influenced by its unique molecular structure, which contains both halogen substituents and a hydroxyl group. Here are some key points to consider regarding its solubility:

  • Polar vs. Nonpolar: The presence of the hydroxyl (-OH) group typically increases solubility in polar solvents, such as water, because it can engage in hydrogen bonding.
  • Halogen Effects: The chlorine and iodine atoms can create a pronounced dipole, potentially impacting solubility in various solvents. The electronegativity of these halogens can result in a complex interplay between polarity and solubility.
  • Solvent Compatibility: In general, compounds that are polar or have polar functional groups tend to be more soluble in polar solvents and less so in nonpolar solvents. However, this compound might exhibit limited solubility due to the bulky nature of the halogen atoms.
  • Practical Assessment: Empirical testing in a laboratory setting would be required to determine the definitive solubility characteristics in various solvents.

In summary, while the hydroxyl group suggests a potential for solubility in polar environments, the significant presence of heavy halogens may hinder overall solubility. Therefore, one might conclude that 4-chloro-2,3-diiodo-but-2-en-1-ol has a nuanced solubility profile that merits detailed examination through experimentation.

Interesting facts

Interesting Facts about 4-Chloro-2,3-diiodo-but-2-en-1-ol

4-Chloro-2,3-diiodo-but-2-en-1-ol is a fascinating compound known for its significant implications in various fields of chemistry and industry. Here are some intriguing aspects of this compound:

  • Structural Versatility: The compound belongs to the category of halogenated alcohols, exhibiting a unique structure that includes both chlorine and iodine substituents. This halogenation gives the compound interesting reactivity, making it a valuable intermediate in organic synthesis.
  • Applications in Synthesis: 4-Chloro-2,3-diiodo-but-2-en-1-ol is often used in the synthesis of biologically active molecules. Its reactive halogen groups can easily participate in nucleophilic substitution reactions, facilitating the formation of complex organic structures.
  • Potential in Medicinal Chemistry: The compound's halogen atoms are known to enhance biological activity. Many pharmaceuticals incorporate halogenated components to improve efficacy and selectivity, making this compound a promising candidate for further drug development studies.
  • Environmental Considerations: Like many halogenated compounds, 4-chloro-2,3-diiodo-but-2-en-1-ol must be handled with care due to potential environmental impacts. Understanding its behavior in different environments is crucial for ensuring safety and compliance with regulations.
  • Research Interest: Ongoing studies aim to explore the reactivity and potential applications of this compound in various chemical reactions, including coupling reactions and as a reagent for the synthesis of other halogenated compounds. Chemists are continually discovering new applications that highlight its significance.

In summary, 4-Chloro-2,3-diiodo-but-2-en-1-ol embodies the intersection of reactivity, synthetic utility, and biological potential. Its diverse characteristics make it a subject of interest not only for organic chemists but also for researchers aiming to discover innovative applications in pharmaceuticals and materials science.